I17T (p.Ile17Thr) variant of RAD50 (DNA repair protein RAD50)
I17T (p.Ile17Thr) in RAD50 (DNA repair protein RAD50) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome; Nijmegen breakage syndrome-like disorde. The available variant effect predictions contribute to a CATVariant prioritization score of 0.60 / 1. The record also includes population frequency data, published literature, and structural context.
I17T (p.Ile17Thr) variant details
- p.Ile17Thr
- rs942335090
- ClinGen CA360951050
- ClinVar RCV000537327
- ClinVar RCV005034088
- Uncertain significance
- Hereditary cancer-predisposing syndrome; Nijmegen breakage syndrome-like disorde
- Missense
- Variant Prioritization Score for Impact Estimate 0.604
- CADD 23.40
- PolyPhen-2 0.25
- SIFT 0.28
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome; Nijmegen breakage syndr)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Cited in: A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic… (PMID 25394175)